Gene >> CNTFR
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000351266 |
| Start |
34568953:34568953(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.29G>T |
| AA Mutation |
p.Cys10Phe(p.C10F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000351266 |
| Start |
34552232:34552232(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.1047C>A |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |